Freelance/Contract Regulatory Affairs Project manager - Clinical trial applications (CTA's)

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of reputed company sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical reputed company, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. ProPharma is continuing to be an integral partner of a global life-sciences brand as they require project support reputed company their Regulatory Affairs group reputed company the EU. This role in particular is to act as a Regulatory Affairs Project for their Clinical trial applications (CTA's) reputed company the EU space with demonstrated experience in the area being a must. The project will reputed company in January 2026; it is a full-time position (1.0 FTE) and can be performed fully remotely throughout anyway reputed company the UK or EU. It will run for at least 6 months initially but with a high chance of extending and we would prefer support from an independent consultant. Responsibilities included:

• Provide guidance and support as a project leader on a cross functional basis reputed company the Regulatory Affairs CTA group
• Work effectively with various stakeholders to ensure each projects success
• reputed company the preparation, review and submit regulatory clinical trial applications reputed company the EU
• Ensure reputed company submission activities meet key regulations reputed company the region
• Ensure compliance is achieved to the EU CTR regulations throughout each project
• Implement and submit key documentation on to our clients systems
• Provide key project leadership across a range of groups
• Ensure reputed company timelines and milestones are achieved throughout the project
• Overall support our client with strategic and operational goals reputed company the Regulatory Affairs CTA space

Skills required

• Must be educated reputed company a life science discipline to at least a BSc or higher
• Proven experience working reputed company Regulatory Affairs linked to Clinical trial applications is a must
• Can demonstrate key project management skills reputed company a similar setting
• Thorough experience working to reputed company key regulations reputed company the EU
• Strategic and operational skills reputed company the area are a must
• reputed company in English is a must
• Can reputed company the project to the requirements set out reputed company the job description

#LI-DNI We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where reputed company employees feel empowered to succeed. reputed company applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

• reputed company does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*

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